ENST00000706528.1:n.1536G>T
|
|
|
ENST00000240306.5:c.655G>T
MANE Select
|
ENSP00000240306.3:p.Gly219Cys
|
|
ENST00000240306.4:c.655G>T
|
ENSP00000240306.3:p.Gly219Cys
|
|
ENST00000411890.3:c.439G>T
|
ENSP00000410622.2:p.Gly147Cys
|
|
ENST00000611342.1:c.*525G>T
|
ENSP00000480366.1:n.*525G>T
|
|
NM_001934.3:c.439G>T
|
NP_001925.2:p.Gly147Cys
|
|
NM_138281.2:c.655G>T
|
NP_612138.1:p.Gly219Cys
|
|
XM_011524459.1:c.439G>T
|
XP_011522761.1:p.Gly147Cys
|
|
XM_017024291.1:c.439G>T
|
XP_016879780.1:p.Gly147Cys
|
|
NM_138281.3:c.655G>T
MANE Select
|
NP_612138.1:p.Gly219Cys
|
|
NM_001934.4:c.439G>T
|
NP_001925.2:p.Gly147Cys
|
|